Canonical Allele Identifier: CA2612003158

Gene: KCNQ1

Linked Data

• gnomAD v4: 11-2528169-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2528169A>G , CM000673.2:g.2528169A>G	GRCh38
NC_000011.9:g.2549399A>G , CM000673.1:g.2549399A>G	GRCh37
NC_000011.8:g.2505975A>G	NCBI36
NG_008935.1:g.88179A>G , LRG_287:g.88179A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.216+151A>G	ENSP00000434560.2:n.216+151A>G
ENST00000646564.2:c.477+151A>G	ENSP00000495806.2:n.477+151A>G
ENST00000155840.12:c.477+151A>G MANE Select	ENSP00000155840.2:n.477+151A>G
ENST00000335475.6:c.96+151A>G	ENSP00000334497.5:n.96+151A>G
ENST00000646564.1:c.123+151A>G	ENSP00000495806.1:n.123+151A>G
ENST00000155840.9:c.477+151A>G	ENSP00000155840.2:n.477+151A>G
ENST00000335475.5:c.96+151A>G	ENSP00000334497.5:n.96+151A>G
ENST00000496887.6:c.216+151A>G	ENSP00000434560.1:n.216+151A>G
NM_000218.2:c.477+151A>G , LRG_287t1:c.477+151A>G	NP_000209.2:n.477+151A>G
NM_181798.1:c.96+151A>G , LRG_287t2:c.96+151A>G	NP_861463.1:n.96+151A>G
NM_000218.3:c.477+151A>G MANE Select	NP_000209.2:n.477+151A>G